Canonical Allele Identifier: CA2649903354

Gene: SYT2

Linked Data

• gnomAD v4: 1-202597058-A-AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202597058_202597059insGT , CM000663.2:g.202597058_202597059insGT	GRCh38
NC_000001.10:g.202566186_202566187insGT , CM000663.1:g.202566186_202566187insGT	GRCh37
NC_000001.9:g.200832809_200832810insGT	NCBI36
NG_041776.1:g.118365_118366insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1054-96_1054-95insAC MANE Select	ENSP00000356237.4:n.1054-96_1054-95insAC
ENST00000367267.5:c.1054-96_1054-95insAC	ENSP00000356236.1:n.1054-96_1054-95insAC
ENST00000367268.4:c.1054-96_1054-95insAC	ENSP00000356237.4:n.1054-96_1054-95insAC
NM_001136504.1:c.1054-96_1054-95insAC	NP_001129976.1:n.1054-96_1054-95insAC
NM_177402.4:c.1054-96_1054-95insAC	NP_796376.2:n.1054-96_1054-95insAC
XM_011509192.1:c.1063-96_1063-95insAC	XP_011507494.1:n.1063-96_1063-95insAC
XR_922430.1:n.82_83insGT
XM_011509192.2:c.1063-96_1063-95insAC	XP_011507494.1:n.1063-96_1063-95insAC
XM_017000309.2:c.1234-96_1234-95insAC	XP_016855798.1:n.1234-96_1234-95insAC
XM_017000310.2:c.1225-96_1225-95insAC	XP_016855799.1:n.1225-96_1225-95insAC
XM_017000311.2:c.1063-96_1063-95insAC	XP_016855800.1:n.1063-96_1063-95insAC
XM_017000312.1:c.1063-96_1063-95insAC	XP_016855801.1:n.1063-96_1063-95insAC
XM_017000313.1:c.1054-96_1054-95insAC	XP_016855802.1:n.1054-96_1054-95insAC
NM_177402.5:c.1054-96_1054-95insAC MANE Select	NP_796376.2:n.1054-96_1054-95insAC